Canonical Allele Identifier: CA1622225773
Gene: BTBD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38398208G= , CM000668.2:g.38398208G= GRCh38
NC_000006.11:g.38365984G= , CM000668.1:g.38365984G= GRCh37
NC_000006.10:g.38473962G= NCBI36
NG_016545.1:g.246941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000481247.6:c.1155-53115C= MANE Select ENSP00000418751.1:n.1155-53115C=
ENST00000649492.1:c.1155-53115C= ENSP00000497066.1:n.1155-53115C=
ENST00000314100.10:c.951-53115C= ENSP00000323408.6:n.951-53115C=
ENST00000328403.10:c.*63-53115C= ENSP00000328328.6:n.*63-53115C=
ENST00000419706.6:c.1064+4609C= ENSP00000415365.2:n.1064+4609C=
ENST00000481247.5:c.1155-53115C= ENSP00000418751.1:n.1155-53115C=
NM_001099272.1:c.1155-53115C= NP_001092742.1:n.1155-53115C=
NM_001172418.1:c.1064+4609C= NP_001165889.1:n.1064+4609C=
NM_052893.1:c.1155-53115C= NP_443125.1:n.1155-53115C=
NM_152733.2:c.951-53115C= NP_689946.2:n.951-53115C=
XM_005248841.2:c.1155-53115C= XP_005248898.1:n.1155-53115C=
XM_011514279.1:c.1155-53115C= XP_011512581.1:n.1155-53115C=
XM_011514281.1:c.1155-52938C= XP_011512583.1:n.1155-52938C=
XM_011514279.3:c.1155-53115C= XP_011512581.1:n.1155-53115C=
XM_011514281.3:c.1155-52938C= XP_011512583.1:n.1155-52938C=
NM_001099272.2:c.1155-53115C= MANE Select NP_001092742.1:n.1155-53115C=
NM_052893.2:c.1155-53115C= NP_443125.1:n.1155-53115C=
NM_001172418.2:c.1064+4609C= NP_001165889.1:n.1064+4609C=
NM_152733.3:c.951-53115C= NP_689946.2:n.951-53115C=